Canonical Allele Identifier: CA346210069

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598404A>T (hg19) ; chr2:g.27375537A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375537A>T , CM000664.2:g.27375537A>T	GRCh38
NC_000002.11:g.27598404A>T , CM000664.1:g.27598404A>T	GRCh37
NC_000002.10:g.27451908A>T	NCBI36
NG_028219.1:g.10208T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.806A>T MANE Select	ENSP00000233575.2:p.Tyr269Phe
ENST00000233575.6:c.806A>T	ENSP00000233575.2:p.Tyr269Phe
ENST00000427123.5:c.*616A>T	ENSP00000405399.1:n.*616A>T
ENST00000440760.5:c.*651A>T	ENSP00000399727.1:n.*651A>T
ENST00000453453.1:c.*333A>T	ENSP00000401922.1:n.*333A>T
ENST00000493711.1:n.523A>T
ENST00000537606.5:c.731A>T	ENSP00000439208.1:p.Tyr244Phe
NM_001267059.1:c.770A>T	NP_001253988.1:p.Tyr257Phe
NM_001267060.1:c.731A>T	NP_001253989.1:p.Tyr244Phe
NM_001267061.1:c.746A>T	NP_001253990.1:p.Tyr249Phe
NM_014748.3:c.806A>T	NP_055563.1:p.Tyr269Phe
NR_049782.1:n.1179A>T
NR_049783.1:n.1152A>T
NR_049784.1:n.1128A>T
NR_049785.1:n.1061A>T
NR_049786.1:n.1010A>T
NR_049787.1:n.861A>T
NR_049788.1:n.791A>T
XM_011533203.1:c.164A>T	XP_011531505.1:p.Tyr55Phe
XM_011533203.2:c.164A>T	XP_011531505.1:p.Tyr55Phe
XM_017005405.2:c.164A>T	XP_016860894.1:p.Tyr55Phe
NM_014748.4:c.806A>T MANE Select	NP_055563.1:p.Tyr269Phe
NM_001267059.2:c.770A>T	NP_001253988.1:p.Tyr257Phe
NM_001267061.2:c.746A>T	NP_001253990.1:p.Tyr249Phe
NR_049782.2:n.1059A>T
NR_049783.2:n.1032A>T
NR_049784.2:n.1008A>T
NR_049785.2:n.941A>T
NR_049786.2:n.890A>T
NR_049787.2:n.741A>T
NR_049788.2:n.671A>T
NM_001267060.2:c.731A>T	NP_001253989.1:p.Tyr244Phe